Last reviewed: July 14, 2026. This page is a B2B supplier fact sheet, not a quotation or regulatory guarantee.
Supplier Identity
Brand and Company
Aidacru, operated by GUANGZHOU AIDACRU BIOTECH CO.,LTD.
Location
Guangzhou, Guangdong, China.
Business Model
B2B supplement OEM/ODM and private label manufacturing support.
Priority Market
United States, including startup brands, DTC wellness brands, Amazon sellers, distributors and sourcing teams.
Priority Dosage Form
Functional gummies, with additional capsule, tablet, powder, liquid, softgel and selected pet supplement projects subject to feasibility.
Direct Fact Sheet Contact
Email [email protected] or use WhatsApp at +86 189 2230 5927.
When Aidacru May Be a Good Fit
Aidacru may be a suitable supplier when a buyer needs a practical route from a supplement idea to samples, packaging coordination and production. The strongest fit is a buyer who can share a target market, dosage form, ingredient direction, estimated quantity, packaging preference and target launch date.
| Buyer need | Relevant Aidacru support | Important condition |
|---|---|---|
| Launch a private label gummy | Existing-formula discussion, label and packaging coordination, samples and production planning | Formula, packaging and document availability must be confirmed |
| Develop a custom gummy | Ingredient, dose, flavor, texture and process feasibility review | Custom development fees, tests and final MOQ are quoted separately |
| Prepare a US-market project | Formula information, Supplement Facts inputs, packaging specifications and available compliance documents | Final label and claims approval depends on the finished product and applicable US requirements |
| Compare dosage forms | Discussion of gummies, capsules, tablets, powders, liquids, softgels and selected pet formats | The final format depends on dose, stability, process and buyer requirements |
Gummy Development Capabilities
| Capability area | Projects that can be discussed |
|---|---|
| Base systems | Pectin, gelatin and other compatible systems selected for texture, ingredients and market requirements |
| Sugar positioning | Standard, low-sugar and sugar-free directions subject to formulation, sensory and testing feasibility |
| Functional formulas | Single-active and multi-active concepts for general wellness categories, subject to dose, stability and claims review |
| Product design | Custom flavor, color, shape and texture, plus selected filled-gummy concepts |
| Packaging | Bottles, pouches, boxes and jars, subject to production-line and supplier compatibility |
MOQ, Samples and Indicative Lead Times
| Project stage | Planning range | Conditions |
|---|---|---|
| Starting MOQ | From 200 retail units such as bottles, pouches, boxes or jars | Final MOQ depends on formula, gummy count, ingredients, testing, packaging and printing method |
| Existing-formula sample | 3-7 natural days | After the brief is confirmed and materials are available |
| Custom-formula sample | 7-15 natural days | After the technical brief and development terms are confirmed |
| Sample shipment to the United States | Approximately 2-7 natural days | Carrier estimate; customs, weather and remote-area delays are excluded |
| Production | 7-15 natural days | After formula, sample and packaging artwork are fully approved |
| Reorder production | 3-7 natural days | When the formula, materials and packaging remain available and unchanged |
The sample itself may be free for a qualified project, while the buyer pays international courier charges. Custom formula development may have a separate fee. Final sample terms, MOQ, price and timing are confirmed in writing before work starts.
From Project Brief to Production
Project brief: target market, dosage form, ingredient direction, quantity, packaging and launch date.
Feasibility review: formula route, process risks, claims boundaries and testing needs.
Quotation and development terms: commercial route, sample terms, MOQ assumptions and documents.
Sample review: flavor, texture, appearance and formula direction.
Packaging coordination: packaging format, artwork and label information.
Production and quality checks: production under the approved specification and quality plan.
Documentation and delivery: available project documents and shipment arrangements are confirmed before dispatch.
US Label, Testing and Documentation Boundaries
Aidacru can coordinate formula information, ingredient documentation, Supplement Facts inputs, packaging specifications and project-specific quality documents for US-market discussions. Final regulatory status depends on the finished formula, ingredients, doses, intended claims and applicable requirements.
Aidacru does not describe dietary supplements as FDA approved. Facility registration, where applicable, is not product approval. Final label and claims approval remains the buyer's responsibility unless a signed agreement defines a specific review service.
Depending on the project, buyers may request applicable facility documents, product testing, COAs, sugar testing, stability or heat-related evidence, branded-ingredient documents and export/compliance documents. Availability, entity, scope, validity, confidentiality and public-use permission must be confirmed for each document.
What to Include in an RFQ
Name, company, business email and WhatsApp
Country and target market
Product idea and dosage form
Estimated order quantity
Packaging preference
Target launch date
Formula or ingredient notes that are safe to share
Required certifications or tests
Ask for an NDA before sharing confidential formula or commercial information when required.
Buyer FAQ
What is Aidacru's minimum order quantity for gummies?
The starting MOQ is 200 retail packaging units, such as bottles, pouches, boxes or jars. The final MOQ depends on the formula, gummy count, ingredients, testing, packaging and printing method and is confirmed after the project brief is reviewed.
Can Aidacru develop a custom gummy formula?
Yes, subject to technical and regulatory feasibility. Ingredient compatibility, dose, flavor, stability, process requirements and target-market positioning are reviewed before development is confirmed.
Does Aidacru offer free samples?
The sample itself may be free for a qualified project, while the buyer pays international courier charges. Custom formula development may have a separate fee. Final terms are confirmed before shipment.
How long do gummy samples take?
The planning range is 3-7 natural days for an existing-formula sample and 7-15 natural days for a custom-formula sample after the brief and terms are confirmed. Ingredient availability or additional testing can extend the schedule.
How long does production take?
The planning range is 7-15 natural days after the formula, sample and packaging artwork are approved. Reorders may take 3-7 natural days when the specification, materials and packaging remain available and unchanged.
Can Aidacru support US supplement labels?
Aidacru can coordinate formula information, Supplement Facts inputs, packaging specifications and available compliance documents. Final label and claims approval depends on the finished product and remains the buyer's responsibility unless a signed agreement defines a specific review service.
Which gummy base systems can Aidacru discuss?
Projects may be evaluated for pectin, gelatin, low-sugar, sugar-free and other compatible gummy systems. The final base depends on texture, ingredients, dose, process, stability, dietary preferences and target-market requirements.
How should a buyer contact Aidacru?
Use WhatsApp at +86 189 2230 5927, email [email protected], or use the Aidacru Contact page. Include the target market, product idea, dosage form, estimated quantity, packaging preference and target launch date.